Canonical Allele Identifier: CA1980452528

Gene: NDUFS8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036580_68036583delinsACTT , CM000673.2:g.68036580_68036583delinsACTT	GRCh38
NC_000011.9:g.67804047_67804050delinsACTT , CM000673.1:g.67804047_67804050delinsACTT	GRCh37
NC_000011.8:g.67560623_67560626delinsACTT	NCBI36
NG_007878.1:g.2565_2568delinsACTT , LRG_115:g.2565_2568delinsACTT
NG_017040.1:g.10964_10967delinsACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.620_623delinsACTT MANE Select	ENSP00000315774.5:p.Tyr207=
ENST00000313468.9:c.620_623delinsACTT	ENSP00000315774.5:p.Tyr207=
ENST00000524810.5:c.552_555delinsACTT
ENST00000528492.1:c.182_185delinsACTT	ENSP00000432848.1:p.Tyr61=
ENST00000531282.1:n.472_475delinsACTT
NM_002496.3:c.620_623delinsACTT	NP_002487.1:p.Tyr207=
XM_005274013.1:c.620_623delinsACTT	XP_005274070.1:p.Tyr207=
XM_005274014.1:c.620_623delinsACTT	XP_005274071.1:p.Tyr207=
XM_005274015.1:c.500_503delinsACTT	XP_005274072.1:p.Tyr167=
XM_011545053.1:c.620_623delinsACTT	XP_011543355.1:p.Tyr207=
NM_002496.4:c.620_623delinsACTT MANE Select	NP_002487.1:p.Tyr207=